Sentence examples for partial syntheses from inspiring English sources

Exact(1)

A number of partial syntheses have already been published (e.g., Arnett et al. 2011a; Arnett and Baerwald 2013; Bergström et al. 2013b; Helldin et al. 2012; Lovich and Ennen 2013; Rydell et al. 2012).

Similar(59)

The second reason is that partial synthesis usually allows a very accurate linkage of records.

KCSR and MLAS isolated the -cubebin and prepared the -hinokinin by partial synthesis.

The dibenzylbutyrolactone lignan -hinokinin (HK) was derived by partial synthesis from -cubebin, isolated from the dry seeds of the pepper, Piper cubeba.

In 2002 he completed his Ph.D. studies under the supervision of Prof. B. Kräutler on the topic of a biomimetic partial synthesis of chlorophyll catabolites.

The conversion of NCC methyl esters into NCCs was accomplished through enzymatic hydrolysis involving porcine liver esterase, also concluding the formal partial synthesis of the enantiomers of natural NCCs.

More recently, photo-oxygenation reactions with Zn- or Cd-complexes of methyl pheophorbide a or of methyl pyropheophorbide a or b were found useful and they allowed the partial synthesis of Chl-catabolites found in plants or in a green alga.

-Hinokinin (HK – Figure 1), a dibenzylbutyrolactone lignan, was derived by partial synthesis from -cubebin isolated from the dry seeds of Piper cubeba[ 1] and proved to be a potential candidate for the development of a new drug to treat Chagas' disease [ 2, 3].

The chemical isomerization of pFCC/ epi-pFCC to pNCC/ epi-pNCC also completed the partial synthesis of natural NCCs from the starting Chl a. 42 The critical role of the propionic acid side chain in the FCC-to-NCC isomerization was further demonstrated by study of this type of isomerization reaction with the related FCC methyl esters.

Also another site in the body for the partial synthesis of this vitamin is the cells of the two kidneys.

In this case, the addition of transition metal, namely mercury oxide [9] or lead tetraacetate [16], allows a partial selective synthesis of benzimidazoles.

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